chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119734939119734940CT49GENIChomozygous54082127
7119735737119735738AG37GENIChomozygous54082128
7119737142119737143CT32GENIChomozygous54082129
7119737538119737539AG33GENIChomozygous54082130
7119738820119738821GA17GENIChomozygous54082131
7119739193119739194GA33GENIChomozygous54082132
7119740085119740086TC46GENICpossibly homozygous54082133
7119740147119740148CT28GENICpossibly homozygous54082134
7119740170119740171GA45GENICheterozygous54233069
7119740189119740190CT46GENICheterozygous54082135
7119740285119740286CG33GENICheterozygous54233071
7119740421119740422CT30GENICheterozygous54507685
7119740501119740502GA21GENIChomozygous54082136
7119741029119741030TTG15GENICheterozygous54082137
7119741029119741030TTGTG15GENICheterozygous54233073
7119741030119741031GGT20GENIChomozygous54082138